A-046
Atropine solution
1.0 mg/mL in acetonitrile, ampule of 1 mL, certified reference material, Cerilliant®
Synonym(s):
Atropine solution
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About This Item
Empirical Formula (Hill Notation):
C17H23NO3
CAS Number:
Molecular Weight:
289.37
UNSPSC Code:
41116107
NACRES:
NA.24
Recommended Products
grade
certified reference material
form
liquid
feature
SNAP-N-SPIKE®. SNAP-N-SHOOT®
packaging
ampule of 1 mL
manufacturer/tradename
Cerilliant®
concentration
1.0 mg/mL in acetonitrile
technique(s)
gas chromatography (GC): suitable
liquid chromatography (LC): suitable
application(s)
clinical testing
format
single component solution
storage temp.
−20°C
InChI
1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3
InChI key
RKUNBYITZUJHSG-UHFFFAOYSA-N
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General description
A Certified Spiking Solution® suitable for use as starting material in calibrators or controls for a variety of LC/MS or GC/MS applications from clinical toxicology to forensic analysis and pharmaceutical research. Atropine is a pharmaceutical drug used for treatment of cardiac conditions.
For the analysis of the phytotoxins. Tropane alkaloid.
For the analysis of the phytotoxins. Tropane alkaloid.
Application
- Atropine sulfate solution: Study conducted a systematic review and meta-analysis on the effectiveness of atropine in managing sialorrhea, highlighting its use as a muscarinic antagonist reagent in clinical settings, providing critical insights for pharmacological research atropine applications (Yellepeddi et al., 2024).
- Pharmacological research atropine: The clinical pharmacokinetics of an atropine oral gel formulation were studied in healthy volunteers, underscoring its importance in acetylcholine receptor studies and its application in developing pharmacokinetic profiles for pharmaceutical research (Parrot et al., 2024).
- Atropine as a muscarinic antagonist in pharmacological research: The study discussed the utility of plant alkaloids, including atropine, in treating eye diseases, illustrating atropine′s role as a vital ophthalmic research chemical and its broader implications in medical research (Lorrai et al., 2024).
- High purity atropine solution for biochemical studies: The study developed a new method for solvent suppression in pure shift NMR, enhancing the understanding of atropine′s interactions at the molecular level, which is crucial for advancing analytical standards for delta8-THC and related compounds in scientific research (Gates et al., 2024).
Legal Information
CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
CERTIFIED SPIKING SOLUTION is a registered trademark of Cerilliant Corporation
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
35.6 °F - closed cup
Flash Point(C)
2 °C - closed cup
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Marija Lukac et al.
European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie, 23(1), 80-84 (2013-02-05)
Evaluation of the effectiveness of oral atropine versus surgical therapy for hypertrophic pyloric stenosis (HPS). A total of 66 consecutive patients with HPS were treated at the University Children's Hospital between January 2006 and December 2011. The diagnosis was initially
Yu-Wen Cheng et al.
International journal of medicinal mushrooms, 15(3), 277-286 (2013-05-15)
In our previous research, Cordyceps militaris (CM) had a hypoglycemic effect in normal rats. In this study we wanted to elucidate whether CM also had an effect on diabetic rats. Twelve rats with streptozotocin-induced diabetes were separated randomly into 2
A I Strelnikova et al.
Bulletin of experimental biology and medicine, 154(2), 180-183 (2013-01-19)
Acetylcholine (5.5×10(-10)-5.5×10(-6)M) accelerated erythrocyte agglutination in men, non-pregnant women in follicular phase of the menstrual cycle, and pregnant women in the first trimester. The effect was blocked with atropine (5.5×10(-6)M). Acetylcholine had no effect on the rate of erythrocyte agglutination
Yoshizumi Takemura et al.
American journal of physiology. Lung cellular and molecular physiology, 304(6), L428-L437 (2013-01-08)
We and others have shown that epithelial Na(+) channels (ENaC) in alveolar type 2 (AT2) cells are activated by β2 agonists, steroid hormones, elevated oxygen tension, and by dopamine. Although acetylcholine receptors (AChRs) have been previously described in the lung
F Aura Kullmann et al.
Life sciences, 92(12), 733-739 (2013-02-13)
To determine if the muscarinic agonist, bethanechol, inhibits the non-cholinergic, atropine-resistant (i.e. putatively purinergic) component of naturally occurring (i.e. reflexogenic) bladder contractions in vivo in the rat, as previously described in vitro. Our second aim was to determine if elevation
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